Judith Atkins

Judith joined Medicago in 2019 bringing over 20 years Regulatory Affairs experience in the Pharmaceutical and Biotech industry. She is a seasoned leader with a proven ability to lead and advise multidisciplinary product development teams from “test-tube” to licensure and beyond.

Creative and pragmatic, Judith combines diverse and deep knowledge of CMC, Clinical and Nonclinical regulatory requirements to move products and projects efficiently through their life cycle while ensuring quality and retaining focus on the customers.

Judith has exceptional organizational and interpersonal skills and is driven by her willingness of maximizing efficiency and delivering continuous process and product improvements.